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Article

Changes in Physical Performance among Community-Dwelling Older Adults in Six Years

by
Darlise Rodrigues dos Passos Gomes
1,*,
Leonardo Pozza Santos
2,
Maria Cristina Gonzalez
1,
Edgar Ramos Vieira
3 and
Renata Moraes Bielemann
1,4
1
Post-Graduate Program in Food and Nutrition, Federal University of Pelotas, Pelotas 96075-630, Brazil
2
Department of Nutrition, Federal University of Pelotas, Pelotas 96075-630, Brazil
3
Department of Physical Therapy, Florida International University, Miami, FL 33199, USA
4
Post-Graduate Program in Epidemiology, Federal University of Pelotas, Pelotas 96020-220, Brazil
*
Author to whom correspondence should be addressed.
Int. J. Environ. Res. Public Health 2023, 20(8), 5579; https://doi.org/10.3390/ijerph20085579
Submission received: 16 March 2023 / Revised: 13 April 2023 / Accepted: 17 April 2023 / Published: 19 April 2023
(This article belongs to the Special Issue Physical Therapy in Geriatrics)

Abstract

:
Changes in physical performance (PP) occur with aging, and understanding the magnitude of these changes over time is important. This study evaluated changes in Gait Speed (GS) and Timed Up and Go (TUG) performance and their association with related factors among community-dwelling older adults over a period of five to six years. A cohort study of 476 older adults with baseline assessment conducted in 2014 and reassessment in 2019–2020 was carried out. Associations between PP changes over time and sociodemographic, behavioral, and health variables were evaluated using mixed linear models. Approximately 68% of the participants declined PP; 20% had no relevant change in GS and 9% in TUG time (sustained PP); 12% increased GS, and 23% decreased TUG time (improved PP). Being male (p = 0.023), living without a partner/separated (p = 0.035), higher education (p = 0.019), and alcohol consumption in the prior month (p = 0.045) were associated with decreased GS, while older age (p < 0.001), having lower socioeconomic status (p < 0.004), physical inactivity (p = 0.017), and being overweight (p = 0.007) were associated with increased TUG time. PP declined for most participants. Factors most strongly associated with PP decline are non-modifiable. The high prevalence of PP decline over time signals the importance of including physical tests in yearly health assessments.

1. Introduction

Physical performance (PP) is a critical health indicator for older adults [1]. Decline in PP is associated with frailty, sarcopenia, disability, cognitive decline, falls, hospitalization, and higher mortality risk [1,2,3,4]. PP changes occur with aging as a dynamic process. The start and magnitude of decline differ between individuals, type of PP test, and setting [5,6,7]. Aging-related declines in cardiovascular, musculoskeletal, and neuromuscular systems’ function result in progressive loss of muscle mass and strength. Sociodemographic, lifestyle (e.g., diet quality and physical activity levels), depressive symptoms, multimorbidity, and nutritional status contribute to these changes [2,3,6,8,9,10]. However, further understanding of the factors associated with PP changes over time in community-dwelling older adults is needed to plan optimal prevention strategies.
Recent studies assessing PP trajectories are based on the categorization of physical performance tests (PPTs) according to cut-off points, which can be useful to identify mobility disorders. However, even if individuals are above the low PP threshold, declines in performance have clinical and practical implications, and identifying these changes can contribute to early diagnosis and implementation of preventive measures in a timely manner [7,11,12,13,14,15]. Thus, understanding these changes over time and factors associated with PP decline is important.
Longitudinal studies are scarce in middle and low-income countries in Latin America. Considering the sociodemographic effects on PP changes, additional studies in these countries are needed to elucidate and to direct public policies to help sustain the health of the older adults. Gait Speed (GS) is recognized as the best test to estimate overall health condition [1]. Although walking speed is the main component of the Timed Up and Go (TUG), it also assesses balance and strength, predicting the risk of falls [8,16]. Moreover, these tests are valid to measure the risk of negative outcomes such as physical disability, cognitive decline, falls, institutionalization, and mortality in older adults [1,2,3,4]. Therefore, this study evaluated changes in the GS and TUG time and associated factors among community-dwelling older adults in Brazil over five to six years of follow-up.

2. Materials and Methods

2.1. Study Population and Participant Recruitment

The study included participants of the Longitudinal Study of Older Adults Health—an ongoing longitudinal cohort study called “COMO VAI?”—Consórcio de Mestrado Orientado para Valorização da Atenção ao Idoso (Master’s Consortium Oriented for the Appreciation of Older Adults Care) initiated in 2014. Inclusion criteria were to be community-dwelling, age ≥ 60 years, and living in the urban area of the city of Pelotas, RS, Brazil (~330,000 inhabitants, 93% urban area) [17]. Those individuals unable to answer the questionnaire due to mental incapacity or who did not have a caregiver to assist them during the interview were not included in the study. For this study, the older adults who were unable to perform the PPTs in the 2014 and the 2019–2020 follow-up were also excluded. Of the 1451 older adults who met the inclusion criteria and agreed to participate in the study, the present study’s final sample included 476 older adults with available information on the GS and TUG in both periods (2014 and 2019–2020). The number of older adults recruited in 2014, as well as the follow-up rate, the identified deaths, and losses and refusals are presented in Figure 1.
The sample size was calculated based on the study of sarcopenia and frailty in older people from Pelotas. The sample size calculation estimated 1121 individuals, considering the prevalence of sarcopenia of 10%, 95% confidence interval, two percentage points as acceptable error and design effect of 1.10, plus 20% for losses and refusals [18]. For the study on frailty, the sample size calculation estimated 857 individuals, considering the prevalence of the outcome of 30%, 95% confidence interval, four percentage points as acceptable error and design effect 1.5, plus 20% for losses and refusals [19]. The sampling process were described elsewhere [18,19]. In brief, it took place in two stages: initially, 133 census tracts were randomly selected from the total of census sectors from Pelotas, based on data from the 2010 Brazilian Demographic Census [17]. In the second stage, 31 households were systematically selected per sector to enable the identification of at least 12 older adults in each one, based on a prior estimate of 0.43 older adult/household. It resulted in 1844 individuals being eligible to take part in the study.
Between January and August 2014, household interviews were carried out, in which a structured questionnaire was applied investigating general aspects related to the health of the older people, as well as sociodemographic variables. PPTs (GS and TUG) and anthropometric measurements were assessed by previously trained and standardized interviewers. In 2016–2017, a new phase of telephone/home interviews was carried out, in addition to monitoring mortality. From September 2019 to March 2020, a new and entirely home-based follow-up was carried out. In this follow-up, interviews were conducted and the PPTs measurements applied in 2014 were repeated. However, the third phase of the study needed to be interrupted due to the COVID-19 pandemic. From 900 individuals targeted to be interviewed in the 2019–2020 follow-up, 537 were actually followed. This study uses data from the first and third interviews of the participants of the “COMO VAI?” study.
The study was conducted according to the guidelines of the Declaration of Helsinki and approved by the Federal University of Pelotas Research Ethics Board (protocol code 472.357/2013 and 1.472.959/2016). Informed consent was obtained from all subjects involved in the study.

2.2. Assessment and Categorization of Physical Performance

PP was evaluated using GS and TUG. Both physical tests were performed twice, and the best performance was used for analysis. Walking aids were permitted if needed, but no caregiver assistance was allowed. GS was assessed by recording the time needed to walk a 4 m linear path without obstacles, using a stopwatch [2]. Before the test, individuals were instructed to walk at fastest speed, without running. The test was performed at the individual’s home on flat ground. Speed was calculated in m/s. TUG performance was assessed as the time in seconds the subjects took to rise from a chair, walk three meters without obstacles quickly but safely, turn around, walk back to the chair and sit down [16]. It was also measured using a stopwatch.
PPTs results were treated as continuous variables (m/s and s) according to time changes in PP tests from 2014 to 2019–2020. Clinically relevant changes were used to classify the performance into categories (declined, sustained, and improved) and they were defined as a variation ≥0.1 m/s in GS, considering previous studies [2,20], and ≥5% in TUG time. Higher TUG time and lower GS indicated PP decline.

2.3. Covariates at Baseline

The potential confounders accounted for in the analysis were age, sex, skin color (observed by the interviewer, considering that this is a marker of social inequality in Brazil), marital status, education level (based on years of education), socio-economic class (according to Associação Brasileira de Empresas de Pesquisa—ABEP [21]), current work status, diet quality (assessed using the Diet Quality Index for the Elderly [22]), leisure-time physical activity level (assessed by the International Physical Activity Questionnaire [23])—those who exercised at least 150 min/week were classified as active—, smoking history, alcohol consumption in the last month, multimorbidity (categorized into “up to four chronic diseases” or “five or more chronic diseases” [24]), presence of depressive symptoms (according to the Geriatric Depressive Scale—GDS-10 [25,26]), and polypharmacy (continuous use of five or more medications [27]). Subjects were classified as low weight, eutrophic, or overweight/obese based on age-specific cut-offs recommended by Lipschitz et al. [28] for Body Mass Index (BMI).

2.4. Statistical Analysis

Pearson’s chi-square test was used to assess possible differences between participants that completed or did not complete the follow-up. Differences in the mean GS and TUG time were analyzed using crude and hierarchically adjusted linear regression models. The variables that were associated with the exposure factor and the outcome were kept in the final adjustment model, considering a significance level of 20%. Associations between PP changes over time and sociodemographic, behavioral, and health variables were evaluated using mixed linear models. The adjustment model used was the same as for linear regression analysis. In all the models, the calculation of the second-order interaction between each exposure factor and the year in which the follow-up took place was included, to assess how much of the change in the PP was due to the analyzed exposure. All analyses were performed using Stata version 16.1 (Stata Corp., College Station, TX, USA). For all tests, a p-value < 0.05 was considered statistically significant.

3. Results

Figure 1 shows the study flow. Most of the participants were female (65.1%), with a mean age of 68 ± 6.7 years. Sociodemographic, behavioral, and health characteristics were similar in both assessments, except for a lower participation in the follow up of those aged 80 years or older at the first interview, and those who were widowers (Table 1).
Approximately 68% of the participants declined in GS and increased TUG time (declined PP). Almost 20% had no relevant change in GS, and 9% had no relevant changes in TUG time (sustained PP). Only 12% and 23% of the sample increased GS and decreased TUG time (improved PP), respectively (Supplementary Figure S1).
The GS and TUG mean times in 2014 and 2019–2020 were 1.04 ± 0.36 m/s vs. 0.85 ± 0.32 m/s and 11.1 ± 8.3 s vs. 12.6 ± 8.0 s, respectively. Supplementary Tables S1 and S2 summarize the GS and TUG mean time values in both assessments, according to the independent variables.
Overall, there was a decline in PP. Being male (p = 0.023), living without a partner/separated (p = 0.035), higher education (p = 0.019), and alcohol consumption in the previous month (p = 0.045) were associated with GS decrease (Table 2 and Figure 2), while older age (p < 0.001), belonging to lower socioeconomic status (p < 0.004), physical inactivity (p = 0.017), and being overweight (p = 0.007) were associated with increased TUG time (Table 2 and Figure 3).

4. Discussion

Our findings showed that most participants presented a PP decline over the time of the study. Being male was the factor most strongly associated with GS decline and older age was the factor most strongly associated with TUG time increase. The PP decline among older people is a widely recognized phenomenon and can be attributed in part to aging-related declines in cardiovascular, musculoskeletal, and neuromuscular systems’ function, resulting in progressive loss of muscle mass and strength [2,3,6,8].
To the best of our knowledge, this is the first study to examine PP changes among community-dwellers in low- or middle-income countries according to clinically significant changes in PPTs, which makes it difficult to compare our results. However, a 4-year longitudinal study of 3018 community-dwelling older Chinese found an yearly decline in GS (−0.019 m/s/year in women and −0.025 m/s/year in men) over 4 years (−8.2% in men and −9.0% in women) [11]. Pinter et al. (2018) [29] evaluated the change in GS between the ages of 73 and 76 and found that 24% of the community-dwelling older people showed a significant clinical decline. The authors assumed the same measure (≥0.1 m/s) used in our study, but by year. Nevertheless, there is a growing number of studies evaluating PP trends or trajectories in different countries such as The Netherlands [7], Switzerland [12], Sweden [13], China [14], and Japan [15]. However, they require at least three measurements over time. Thus, both the definition of “low performance” and “meaningful decline” are variable across studies [30]. Some are based on sampling distributions (e.g., quartiles), others on external criteria (e.g., GS <0.8 m/s) and others on changes over time (e.g., ≥0.05 m/s) [29,31,32]. In our study we obtained similar results for both tests regarding the PP decline, in consonance with results from other studies using GS and TUG test [8,33,34].
On the other hand, an important proportion of participants exhibited a sustained or improved PP. Most of the participants (61%) were 60–70 years old in the baseline interview, which may explain the percentages of stability found in our study. The age between 80–85 is the period where the greatest changes in health are observed, affecting GS and TUG, as shown in previous studies [11,35,36]. This coincides with Lee et al. (2019), who observed stable trajectories in GS among community-dwelling older adults aged 65–84 years [36]. A PP increase may be observed due to changes in the participants’ lifestyle during this period. In this sense, numerous interventions regarding physical activity have shown progress in mobility, strength, and/or balance among healthy or community-dwelling older people [37,38]. Although both tests (GS and TUG) were used aiming to assess PP, these two tests evaluate different dimensions, since the TUG considers, in addition to mobility, strength and dynamic balance, and each of the dimensions is impacted in a different way with aging [7,36].
We assess PP through two widely recommended tests because they are simple, cheap, and fast measures, especially in community setting [8,33]. In our study, we observed that approximately a quarter of the participants (27%) did not have agreeing tests (data not shown), reinforcing the importance of using more than one PPTs in a complementary way to better target the necessary interventions among older people.
Our results showed that older age, being male, low socioeconomic status, higher education, living alone/separated, physical inactivity, being overweight, and alcohol consumption in the last month were associated with a PP decline. This set of factors, except higher education, is widely recognized in the literature and it is associated with worse indicators of overall health of older adults, including PP [9,10,30,31,39,40]. Considering that the PP decline is associated with numerous negative outcomes, which can be reduced by intervening on potentially modifiable risk factors, studies have shown consistent results related to the major influence of low physical activity and obesity on PP decrease [9,10,30,39,41,42]. In addition, obesity can coexist with lower muscle mass, favoring the emergence of a condition called sarcopenic obesity, negatively related to PP, explained by factors such as fatty infiltration in the muscles [43]. Regarding the level of education, older adults with higher education had a more pronounced decline in GS, probably due to the fact that they exhibited higher means both in 2014 and in 2019. In part, this can be explained by the cut-off point used to classify significant clinical change in GS, making it easier to identify variation in the faster ones and not in the slower ones. Previous study with U.S Chinese older adults found that higher education was one of the main factors associated with a faster rate of decline in all PP measures evaluated (including chair stand, tandem stand, and timed walk) [31].
Evidence points out that multicomponent training programs (MCT) are one of the most effective interventions to improve PP in older people [44]. An experimental study with 25 older adults showed that physical and cognitive status remained enhanced two years later compared to baseline, except for lower-limb strength. Among the evaluated physical functions, it was verified that strength and cardiovascular fitness were more sensitive to detraining, whilst agility proved to have larger training retentions [45]. A Spanish study observed positive effects of MCT in 106 older adults with or at greater risk of frailty, whereas 4-months of detraining caused a drop of variables related to functional capacity and frailty [46]. In this sense, the effects of detraining should be considered, although we emphasize the originality of our study, which aimed to understand how this occurs on a large scale, among community-dwelling older people in free-living, that is, exposed to common life habits (which include low practice of physical activity).
It is important to report that the most important exposures related to the PP decline are considered as non-modifiable factors, since advanced age and being male were the factors most strongly associated with TUG time increase and GS decline, respectively, in our cohort. As previously described, balance and strength are necessary to perform the TUG and it is known that balance worsens from the age of 70 and muscle strength reduces around 30% among individuals at this age [47]. Furthermore, advanced age represents an accumulation of intrinsic and extrinsic factors associated with aging that can contribute to the PP decline, as verified in a cross-sectional study among elders aged 80 years or older in Vietnam with GS assessed by 4-m walk test [48]. This finding is in line with other studies reporting PP declines in older adults [11,31,32,48], except for a recent study that found a meaningful increase in GS over 10 years of follow-up among over 1000 Swiss older adults [12]. Interestingly, this study evaluated whether new cohorts of older people are in better health than previous ones. The authors mention that the significant improvement observed in physical performance tests over the last decade may be a reflection of a new generation of individuals who enter into old age with better PP, probably due to a greater concern with health.
Even though men showed a more accentuated PP decline, they exhibited better performance in both tests and evaluations (2014 and 2019) than women: 1.16 vs. 1.03 m/s (baseline) and 0.90 vs. 0.83 m/s (follow-up) for GS, respectively, and 9.2 vs. 11.9 s (baseline) and 11.2 vs. 12.9 s (follow-up) for TUG time, corresponding to a greater percentage of variation in physical test measures between men (22.4% for GS and 29.3% for TUG) compared to women (19.4% for GS and 15.2% for TUG). Regarding the health-disease-disability process, men tend to have a worse general health condition, due to less access to health services and low adherence to the treatment of chronic conditions, which is reflected in lower life-expectancy [49]. On the contrary, studies have observed that GS decline was faster in women than in men [50,51]. This discrepancy may be due to differences in walking protocols (distance, usual pace, acceleration, and deceleration phase). Furthermore, Sialino et al. (2021) found that GS determinants were similar between genders, but the lower GS observed among women may be due to the fact that they have both greater sensitivity (higher BMI and lower level of physical activity) and greater exposure (low schooling, living alone, more chronic diseases) to GS determinants than men [52].
We highlight that this study has a longitudinal design and a robust statistical model of adjustment considering a large number of factors potentially associated with PP. In addition, the use of two widely recommended PPTs allows the comparison with populations from different countries. This study provides data on PP in community-dwelling older people, filling a gap related to the scarcity of research in Brazil and Latin America in this field.
Our study has several limitations. First, the assessment of PP was limited to two PPTs, leaving other important dimensions uncovered, such as specific measures of balance, endurance, and strength. Second, we considered a set of factors potentially associated with PP changes among older adults, as indicated in previous studies. However, other not investigated variables may contribute to the decline. Our group is planning another follow-up wave so that we can assess other factors, including the impact of the pandemic on PP. Third, the point used to determine a significant decline in GS can be troublesome, leading to classification errors. It may be easier to identify variation in the fastest but not in the slowest ones. For example, in individuals with normal GS at baseline (1.0 m/s), a decline of 0.1 m/s represents a variation of 10%. On the other hand, those with slow GS at baseline and who also presented 10% variation in the test were not classified with a decline in PP (from 0.80 m/s to 0.72 m/s, for example). For individuals with slow GS, 0.1 m/s represents a greater variation. However, it should be noted that our study used the value described in the literature for significant clinical change in PP [2,20]. Finally, the interruption of follow-up in 2020 due to the COVID-19 pandemic reduced participation of the older people; however, it did not affect the detection of significant associations in this sample [53].
Future studies evaluating other dimensions of PP will help to understand the changes related to the aging, in consonance with a recent study that observed little overlap between the trajectories of different PPTs, suggesting a combination of measures, especially in the assessment of younger older people [7]. Longitudinal studies evaluating PP changes in older people from the perspective assumed in this study are needed to identify an earlier PP decline, allowing preventive measures to be taken in a timely manner.
Our findings have practical implications. The high prevalence of PP decline reinforces the importance of including PPTs early in the health assessment routine of the older people aiming to better target interventions preventing mobility disorders, not only among those who already have low performance, but also among those that show decline. Primary care providers and other health professionals are important in early identification and timely intervention. Preventive clinical measures in all health care settings need to be engaged with public policies to allow community spaces that ensure healthy and active aging.

5. Conclusions

This study showed that PP declined for most participants. Being male was the factor most strongly associated with GS decline, and age was the factor most strongly associated with TUG time increase over a five- to six-year period. The high prevalence of PP decline over time signals the importance of including physical tests in yearly health assessments.

Supplementary Materials

The following are available online at https://www.mdpi.com/article/10.3390/ijerph20085579/s1, Figure S1: Change in physical performance tests-Gait Speed (GS) and Timed Up and Go (TUG)-from 2014 to 2019-20 of the older people in the COMO VAI? Study, Table S1: Mean Gait Speed (GS) in 2014 and 2019 according to sociodemographic, behavioral and health-related variables of the older adults in the COMO VAI? study. N = 476. Pelotas, Brazil, Table S2: Mean Timed Up and Go (TUG) in 2014 and 2019 according to sociodemographic, behavioral and health-related variables of the older adults in the COMO VAI? study. N = 476. Pelotas, Brazil.

Author Contributions

Conceptualization, D.R.d.P.G., L.P.S., M.C.G., E.R.V. and R.M.B.; formal analysis, D.R.d.P.G., L.P.S. and R.M.B.; funding acquisition, D.R.d.P.G., L.P.S., M.C.G., E.R.V. and R.M.B.; methodology, D.R.d.P.G., L.P.S., M.C.G. and R.M.B.; writing—original draft, D.R.d.P.G., L.P.S. and R.M.B.; writing—review and editing, M.C.G. and E.R.V. All authors have read and agreed to the published version of the manuscript.

Funding

This study is part of the Longitudinal Study of Older Adults Health—Continuing the ‘‘COMO VAI?’’ Study. The baseline (2014) was financed by the Coordination for the Improvement of Higher Education Personnel (CAPES—Aperfeiçoamento de Pessoal de Nível Superior) and individual resources from master’s students. The second wave (2017) was partially financed by the National Council for Scientific and Technological Development (CNPq—Conselho Nacional de Desenvolvimento Científico e Tecnológico). The third wave (2019–2020) was partially financed by CAPES. RMB and MCG are CNPq Research Productivity Fellows. DRPG received a sandwich PhD scholarship from CNPq. ERV received a publication fee waiver at IJERPH.

Institutional Review Board Statement

The study was conducted in accordance with the Declaration of Helsinki and the current legislation of human clinical research of Brazil (Resolution 466/2012). The study protocol was submitted and approved by the Federal University of Pelotas Research Ethics Board (protocol code 472.357/2013 and 1.472.959/2016).

Informed Consent Statement

Informed consent was obtained from all subjects involved in the study.

Data Availability Statement

The data used in this study can be obtained upon request from the corresponding author.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Middleton, A.; Fritz, S.L.; Lusardi, M. Walking Speed: The Functional Vital Sign. J. Aging Phys. Act. 2015, 23, 314–322. [Google Scholar] [CrossRef] [PubMed]
  2. Abellan Van Kan, G.; Rolland, Y.; Andrieu, S.; Bauer, J.; Beauchet, O.; Bonnefoy, M.; Cesari, M.; Donini, L.M.; Gillette-Guyonnet, S.; Inzitari, M.; et al. Gait speed at usual pace as a predictor of adverse outcomes in community-dwelling older people an International Academy on Nutrition and Aging (IANA) Task Force. J. Nutr. Health Aging 2009, 13, 881–889. [Google Scholar] [CrossRef] [PubMed]
  3. Bortone, I.; Sardone, R.; Lampignano, L.; Castellana, F.; Zupo, R.; Lozupone, M.; Moretti, B.; Giannelli, G.; Panza, F. How gait influences frailty models and health-related outcomes in clinical-based and population-based studies: A systematic review. J. Cachexia Sarcopenia Muscle 2021, 12, 274–297. [Google Scholar] [CrossRef] [PubMed]
  4. Bergland, A.; Jørgensen, L.; Emaus, N.; Strand, B.H. Mobility as a predictor of all-cause mortality in older men and women: 11.8 year follow-up in the Tromsø study. BMC Health Serv. Res. 2017, 17, 22. [Google Scholar] [CrossRef]
  5. Longobucco, Y.; Krumpoch, S.; Lauretani, F.; Angileri, V.; Sieber, C.; Marzetti, E.; Calvani, R.; Cherubini, A.; Landi, F.; Bernabei, R.; et al. Gait characteristics in community-dwelling older persons with low skeletal muscle mass and low physical performance. Aging Clin. Exp. Res. 2022, 34, 1563–1571. [Google Scholar] [CrossRef]
  6. Ferrucci, L.; Cooper, R.; Shardell, M.; Simonsick, E.M.; Schrack, J.A.; Kuh, D. Age-Related Change in Mobility: Perspectives From Life Course Epidemiology and Geroscience. GERONA 2016, 71, 1184–1194. [Google Scholar] [CrossRef]
  7. Hoekstra, T.; Rojer, A.G.M.; van Schoor, N.M.; Maier, A.B.; Pijnappels, M. Distinct Trajectories of Individual Physical Performance Measures Across 9 Years in 60- to 70-Year-Old Adults. J. Gerontol. Ser. A 2020, 75, 1951–1959. [Google Scholar] [CrossRef]
  8. Beaudart, C.; Rolland, Y.; Cruz-Jentoft, A.J.; Bauer, J.M.; Sieber, C.; Cooper, C.; Al-Daghri, N.; Araujo de Carvalho, I.; Bautmans, I.; Bernabei, R.; et al. Assessment of Muscle Function and Physical Performance in Daily Clinical Practice: A position paper endorsed by the European Society for Clinical and Economic Aspects of Osteoporosis, Osteoarthritis and Musculoskeletal Diseases (ESCEO). Calcif. Tissue Int. 2019, 105, 1–14. [Google Scholar] [CrossRef]
  9. Figgins, E.; Choi, Y.-H.; Speechley, M.; Montero-Odasso, M. Associations Between Potentially Modifiable and Nonmodifiable Risk Factors and Gait Speed in Middle- and Older-Aged Adults: Results From the Canadian Longitudinal Study on Aging. J. Gerontol. Ser. A 2021, 76, e253–e263. [Google Scholar] [CrossRef]
  10. Chung, C.-M.; Shin, S.; Lee, Y.; Lee, D.-Y. Determination of the Predictors with the Greatest Influence on Walking in the Elderly. Medicina 2022, 58, 1640. [Google Scholar] [CrossRef]
  11. Auyeung, T.W.; Lee, S.W.J.; Leung, J.; Kwok, T.; Woo, J. Age-associated decline of muscle mass, grip strength and gait speed: A 4-year longitudinal study of 3018 community-dwelling older Chinese: Longitudinal decline of muscle mass and function. Geriatr. Gerontol. Int. 2014, 14, 76–84. [Google Scholar] [CrossRef] [PubMed]
  12. Henchoz, Y.; Büla, C.; von Gunten, A.; Blanco, J.M.; Seematter-Bagnoud, L.; Démonet, J.-F.; Waeber, G.; Nanchen, D.; Santos-Eggimann, B. Trends in Physical and Cognitive Performance Among Community-Dwelling Older Adults in Switzerland. J. Gerontol. Ser. A 2020, 75, 2347–2353. [Google Scholar] [CrossRef] [PubMed]
  13. Vetrano, D.L.; Rizzuto, D.; Calderón-Larrañaga, A.; Onder, G.; Welmer, A.-K.; Bernabei, R.; Marengoni, A.; Fratiglioni, L. Trajectories of functional decline in older adults with neuropsychiatric and cardiovascular multimorbidity: A Swedish cohort study. PLoS Med. 2018, 15, e1002503. [Google Scholar] [CrossRef] [PubMed]
  14. Yang, R.; Xu, D.; Wang, H.; Xu, J. Longitudinal trajectories of physical functioning among Chinese older adults: The role of depressive symptoms, cognitive functioning and subjective memory. Age Ageing 2021, 50, 1682–1691. [Google Scholar] [CrossRef]
  15. Taniguchi, Y.; Fujiwara, Y.; Murayama, H.; Yokota, I.; Matsuo, E.; Seino, S.; Nofuji, Y.; Nishi, M.; Matsuyama, Y.; Shinkai, S. Prospective Study of Trajectories of Physical Performance and Mortality Among Community-Dwelling Older Japanese. GERONA 2016, 71, 1492–1499. [Google Scholar] [CrossRef]
  16. Podsiadlo, D.; Richardson, S. The Timed “Up & Go”: A Test of Basic Functional Mobility for Frail Elderly Persons. J. Am. Geriatr. Soc. 1991, 39, 142–148. [Google Scholar] [CrossRef]
  17. IBGE. Censo 2010 [Internet]. Instituto Brasileiro de Geografia e Estatística. Available online: https://biblioteca.ibge.gov.br/visualizacao/periodicos/93/cd_2010_caracteristicas_populacao_domicilios.pdf (accessed on 6 September 2022).
  18. Barbosa-Silva, T.G.; Bielemann, R.M.; Gonzalez, M.C.; Menezes, A.M.B. Prevalence of sarcopenia among community-dwelling elderly of a medium-sized South American city: Results of the COMO VAI ? study: Sarcopenia prevalence in a South American city. J. Cachexia Sarcopenia Muscle 2016, 7, 136–143. [Google Scholar] [CrossRef]
  19. Farías-Antúnez, S.; Fassa, A.G. Prevalência e fatores associados à fragilidade em população idosa do Sul do Brasil, 2014. Epidemiol. Serv. Saúde 2019, 28, e2017405. [Google Scholar] [CrossRef]
  20. Perera, S.; Mody, S.H.; Woodman, R.C.L.; Studenski, S.A. Meaningful Change and Responsiveness in Common Physical Performance Measures in Older Adults: MEANINGFUL CHANGE AND PERFORMANCE. J. Am. Geriatr. Soc. 2006, 54, 743–749. [Google Scholar] [CrossRef]
  21. ABEP. Critério de Classificação Econômica Brasil Associação Brasileira de Empresas de Pesquisa. 2014. Available online: https://www.abep.org/criterio-brasil (accessed on 20 September 2022).
  22. Gomes, A.P.; Soares, A.L.G.; Gonçalves, H. Baixa qualidade da dieta de idosos: Estudo de base populacional no sul do Brasil. Ciênc. Saúde Coletiva 2016, 21, 3417–3428. [Google Scholar] [CrossRef]
  23. Craig, C.L.; Marshall, A.L.; Sjöström, M.; Bauman, A.E.; Booth, M.L.; Ainsworth, B.E.; Pratt, M.; Ekelund, U.; Yngve, A.; Sallis, J.F.; et al. International Physical Activity Questionnaire: 12-Country Reliability and Validity. Med. Sci. Sport. Exerc. 2003, 35, 1381–1395. [Google Scholar] [CrossRef] [PubMed]
  24. Montes, M.C.; Bortolotto, C.C.; Tomasi, E.; Gonzalez, M.C.; Barbosa-Silva, T.G.; Domingues, M.R.; Bielemann, R.M. Strength and multimorbidity among community-dwelling elderly from southern Brazil. Nutrition 2020, 71, 110636. [Google Scholar] [CrossRef] [PubMed]
  25. Yesavage, J.A.; Brink, T.L.; Rose, T.L.; Lum, O.; Huang, V.; Adey, M.; Leirer, V.O. Development and validation of a geriatric depression screening scale: A preliminary report. J. Psychiatr. Res. 1982, 17, 37–49. [Google Scholar] [CrossRef] [PubMed]
  26. Almeida, O.P.; Almeida, S.A. Short versions of the geriatric depression scale: A study of their validity for the diagnosis of a major depressive episode according to ICD-10 and DSM-IV. Int. J. Geriatr. Psychiatry 1999, 14, 858–865. [Google Scholar] [CrossRef]
  27. Ramos, L.R.; Tavares, N.U.L.; Bertoldi, A.D.; Farias, M.R.; Oliveira, M.A.; Luiza, V.L.; da Silva Dal Pizzol, T.; Arrais, P.S.D.; Mengue, S.S.; Ramos, L.R.; et al. Polifarmácia e polimorbidade em idosos no Brasil: Um desafio em saúde pública. Rev. De Saúde Pública 2016, 50, s1518–s8787. [Google Scholar]
  28. Lipschitz, D.A. Screening for nutritional status in the elderly. Prim. Care 1994, 21, 55–67. [Google Scholar] [CrossRef]
  29. Pinter, D.; Ritchie, S.J.; Gattringer, T.; Bastin, M.E.; del C. Valdés Hernández, M.; Corley, J.; Maniega, S.M.; Pattie, A.; Dickie, D.A.; Gow, A.J.; et al. Predictors of gait speed and its change over three years in community-dwelling older people. Aging 2018, 10, 144–153. [Google Scholar] [CrossRef]
  30. Figgins, E.; Pieruccini-Faria, F.; Speechley, M.; Montero-Odasso, M. Potentially modifiable risk factors for slow gait in community-dwelling older adults: A systematic review. Ageing Res. Rev. 2021, 66, 101253. [Google Scholar] [CrossRef]
  31. Dong, X.; Bergren, S.M.; Simon, M.A. The Decline of Directly Observed Physical Function Performance Among U.S. Chinese Older Adults. J. Gerontol. Ser. A 2017, 72, S11–S15. [Google Scholar] [CrossRef]
  32. Inzitari, M.; Carlo, A.; Baldereschi, M.; Pracucci, G.; Maggi, S.; Gandolfo, C.; Bonaiuto, S.; Farchi, G.; Scafato, E.; Carbonin, P.; et al. Risk and Predictors of Motor-Performance Decline in a Normally Functioning Population-Based Sample of Elderly Subjects: The Italian Longitudinal Study on Aging: Motor-performance decline in older people. J. Am. Geriatr. Soc. 2006, 54, 318–324. [Google Scholar] [CrossRef]
  33. Cruz-Jentoft, A.J.; Bahat, G.; Bauer, J.; Boirie, Y.; Bruyère, O.; Cederholm, T.; Cooper, C.; Landi, F.; Rolland, Y.; Sayer, A.A.; et al. Sarcopenia: Revised European consensus on definition and diagnosis. Age Ageing 2019, 48, 16–31. [Google Scholar] [CrossRef] [PubMed]
  34. Bruyère, O.; Beaudart, C.; Reginster, J.-Y.; Buckinx, F.; Schoene, D.; Hirani, V.; Cooper, C.; Kanis, J.A.; Rizzoli, R.; McCloskey, E.; et al. Assessment of muscle mass, muscle strength and physical performance in clinical practice: An international survey. Eur. Geriatr. Med. 2016, 7, 243–246. [Google Scholar] [CrossRef]
  35. Santoni, G.; Angleman, S.; Welmer, A.-K.; Mangialasche, F.; Marengoni, A.; Fratiglioni, L. Age-Related Variation in Health Status after Age 60. PLoS ONE 2015, 10, e0120077. [Google Scholar] [CrossRef]
  36. Lee, A.; Bhatt, T.; Smith-Ray, R.L.; Wang, E.; Pai, Y.-C. (Clive) Gait Speed and Dynamic Stability Decline Accelerates Only in Late Life: A Cross-sectional Study in Community-Dwelling Older Adults. J. Geriatr. Phys. Ther. 2019, 42, 73–80. [Google Scholar] [CrossRef] [PubMed]
  37. Aartolahti, E.; Lönnroos, E.; Hartikainen, S.; Häkkinen, A. Long-term strength and balance training in prevention of decline in muscle strength and mobility in older adults. Aging Clin. Exp. Res. 2020, 32, 59–66. [Google Scholar] [CrossRef]
  38. Pacheco, T.B.F.; de Medeiros, C.S.P.; de Oliveira, V.H.B.; Vieira, E.R.; de Cavalcanti, F.A.C. Effectiveness of exergames for improving mobility and balance in older adults: A systematic review and meta-analysis. Syst. Rev. 2020, 9, 163. [Google Scholar] [CrossRef]
  39. Laddu, D.R.; Parimi, N.; Stone, K.L.; Lapidus, J.; Hoffman, A.R.; Stefanick, M.L.; Langsetmo, L. Physical Activity Trajectories and Associated Changes in Physical Performance in Older Men: The MrOS Study. J. Gerontol. Ser. A 2020, 75, 1967–1973. [Google Scholar] [CrossRef] [PubMed]
  40. de Almeida Busch, T.; Duarte, Y.A.; Pires Nunes, D.; Lebrão, M.L.; Satya Naslavsky, M.; dos Santos Rodrigues, A.; Amaro, E. Factors associated with lower gait speed among the elderly living in a developing country: A cross-sectional population-based study. BMC Geriatr. 2015, 15, 35. [Google Scholar] [CrossRef]
  41. Calderón-Larrañaga, A.; Hu, X.; Haaksma, M.; Rizzuto, D.; Fratiglioni, L.; Vetrano, D.L. Health trajectories after age 60: The role of individual behaviors and the social context. Aging 2021, 13, 19186–19206. [Google Scholar] [CrossRef]
  42. Hardy, R.; Cooper, R.; Aihie Sayer, A.; Ben-Shlomo, Y.; Cooper, C.; Deary, I.J.; Demakakos, P.; Gallacher, J.; Martin, R.M.; McNeill, G.; et al. Body Mass Index, Muscle Strength and Physical Performance in Older Adults from Eight Cohort Studies: The HALCyon Programme. PLoS ONE 2013, 8, e56483. [Google Scholar] [CrossRef]
  43. Kalinkovich, A.; Livshits, G. Sarcopenic obesity or obese sarcopenia: A cross talk between age-associated adipose tissue and skeletal muscle inflammation as a main mechanism of the pathogenesis. Ageing Res. Rev. 2017, 35, 200–221. [Google Scholar] [CrossRef] [PubMed]
  44. Bull, F.C.; Al-Ansari, S.S.; Biddle, S.; Borodulin, K.; Buman, M.P.; Cardon, G.; Carty, C.; Chaput, J.-P.; Chastin, S.; Chou, R.; et al. World Health Organization 2020 guidelines on physical activity and sedentary behaviour. Br. J. Sport. Med. 2020, 54, 1451–1462. [Google Scholar] [CrossRef] [PubMed]
  45. Blasco-Lafarga, C.; Cordellat, A.; Forte, A.; Roldán, A.; Monteagudo, P. Short and Long-Term Trainability in Older Adults: Training and Detraining Following Two Years of Multicomponent Cognitive—Physical Exercise Training. Int. J. Environ. Res. Public Health 2020, 17, 5984. [Google Scholar] [CrossRef] [PubMed]
  46. Fernández-García, Á.I.; Moradell, A.; Navarrete-Villanueva, D.; Subías-Perié, J.; Pérez-Gómez, J.; Ara, I.; González-Gross, M.; Casajús, J.A.; Vicente-Rodríguez, G.; Gómez-Cabello, A. Effects of Multicomponent Training Followed by a Detraining Period on Frailty Level and Functional Capacity of Older Adults with or at Risk of Frailty: Results of 10-Month Quasi-Experimental Study. J. Environ. Res. Public Health 2022, 19, 12417. [Google Scholar] [CrossRef]
  47. Rogers, M.A.; Evans, W.J. Changes in skeletal muscle with aging: Effects of exercise training. Exerc. Sport Sci. Rev. 1993, 21, 65–102. [Google Scholar] [CrossRef]
  48. Nguyen, A.T.; Nguyen, H.T.T.; Nguyen, H.T.T.; Nguyen, T.X.; Nguyen, T.N.; Nguyen, T.T.H.; Nguyen, A.L.; Pham, T.; Vu, H.T.T. Walking Speed Assessed by 4-Meter Walk Test in the Community-Dwelling Oldest Old Population in Vietnam. J. Environ. Res. Public Health 2022, 19, 9788. [Google Scholar] [CrossRef]
  49. Destro, J.R.; Boing, A.F.; d’Orsi, E. Factors associated to medical consultations by elderly adults in southern Brazil: A population based study. Rev. Bras. Epidemiol. 2014, 17, 692–704. [Google Scholar] [CrossRef]
  50. Coelho-Junior, H.J.; Uchida, M.C.; Gonçalves, I.O.; Calvani, R.; Rodrigues, B.; Picca, A.; Onder, G.; Landi, F.; Bernabei, R.; Marzetti, E. Age- and Gender-Related Changes in Physical Function in Community-Dwelling Brazilian Adults Aged 50 to 102 Years. J. Geriatr. Phys. Ther. 2021, 44, E123–E131. [Google Scholar] [CrossRef]
  51. Melsæter, K.N.; Tangen, G.G.; Skjellegrind, H.K.; Vereijken, B.; Strand, B.H.; Thingstad, P. Physical performance in older age by sex and educational level: The HUNT Study. BMC Geriatr. 2022, 22, 821. [Google Scholar] [CrossRef]
  52. Sialino, L.D.; Schaap, L.A.; van Oostrom, S.H.; Picavet, H.S.J.; Twisk, J.W.R.; Verschuren, W.M.M.; Visser, M.; Wijnhoven, H.A.H. The sex difference in gait speed among older adults: How do sociodemographic, lifestyle, social and health determinants contribute? BMC Geriatr. 2021, 21, 340. [Google Scholar] [CrossRef]
  53. Vargas, P.M.; Schneider, B.C.; Costa, C.S.; César, J.A.; Bertoldi, A.D.; Tomasi, E.; Demarco, F.F.; Gonzalez, M.C.; Bielemann, R.M. Age is the most important factor for change in body mass index and waist circumference in older people in southern Brazil. Nutrition 2023, 109, 111956. [Google Scholar] [CrossRef] [PubMed]
Figure 1. Flowchart of the Longitudinal Study of Older Adults Health: continuing the “COMO VAI?” study. * Number of living older adults located and interviewed before the study was interrupted due to the COVID-19 pandemic; the deaths that occurred until December/2022 were not yet verified by the epidemiological surveillance of Pelotas due to the duration of the pandemic.
Figure 1. Flowchart of the Longitudinal Study of Older Adults Health: continuing the “COMO VAI?” study. * Number of living older adults located and interviewed before the study was interrupted due to the COVID-19 pandemic; the deaths that occurred until December/2022 were not yet verified by the epidemiological surveillance of Pelotas due to the duration of the pandemic.
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Figure 2. Difference in GS between 2014 and 2019 according to sex, marital status, education level, and alcohol consumption of individuals.
Figure 2. Difference in GS between 2014 and 2019 according to sex, marital status, education level, and alcohol consumption of individuals.
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Figure 3. Evolution in terms of TUG time between 2014 and 2019 according to age, economic level, physical activity level, and body mass index (BMI).
Figure 3. Evolution in terms of TUG time between 2014 and 2019 according to age, economic level, physical activity level, and body mass index (BMI).
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Table 1. Sample description according to sociodemographic, behavioral, and health-related characteristics in the 2014 and 2019 years of the COMO VAI? study.
Table 1. Sample description according to sociodemographic, behavioral, and health-related characteristics in the 2014 and 2019 years of the COMO VAI? study.
Complete Sample in 2014Study Sample in 2019
Variablesn= 1451% (95%CI) an = 476% (95%CI) a
Sex
  Female
  Male
Age (completed years)
914
537
63.0 (60.5; 65.4)
37.0 (34.6; 39.5)
310
166
65.1 (60.7; 69.3)
34.9 (30.7; 39.3)
  60–69
  70–79
  80+
756
460
230
52.3 (49.7; 54.9)
31.8 (29.5; 34.3)
15.9 (14.1; 17.9)
289
151
36
60.7 (56.2; 65.0)
31.7 (27.7; 36.1)
7.6 (5.5; 10.3)
Skin color
  White121183.7 (81.7; 85.6)389 81.7 (78.0; 85.0)
  Other than white23616.3 (14.5; 18.3)87 18.3 (15.0; 22.0)
Marital status
  Married/with a partner763 52.7 (50.2; 55.3)286 60.1 (55.6; 64.4)
  Without a partner/separated 225 15.6 (13.8; 17.6)72 15.1 (12.2; 18.6)
  Widow(er)459 31.7 (29.4; 34.2)118 24.8 (21.1; 28.9)
Economic level b
  A/B483 35.2 (32.7; 37.8)161 35.4 (31.1; 39.9)
  C720 52.5 (49.8; 55.1)248 54.5 (49.9; 59.0)
  D/E169 12.3 (10.7; 14.2)46 10.1 (7.7; 13.2)
Education level (completed years)
  None
  1–7
  ≥8
196
782
459
13.6 (12.0; 15.5)
54.4 (51.8; 57.0)
32.0 (29.6; 34.4)
54
270
151
11.4 (8.8; 14.6)
56.8 (52.3; 61.2)
31.8 (27.7; 36.1)
Current work situation
  No (unemployed)1084 80.4 (78.2; 82.4)344 77.0 (72.8; 80.6)
  Yes (employed)264 19.6 (17.6; 21.8)103 23.0 (19.4; 27.2)
Diet quality c
  Low481 33.7 (31.3; 36.2)143 30.2 (26.3; 34.6)
  Average534 37.5 (35.0; 40.0)177 37.5 (33.2; 41.9)
  High411 28.8 (26.5; 31.2)153 32.3 (28.3; 36.7)
Leisure-time physical activity (>150 min/week) d
  No 1133 81.5 (79.3; 83.4)378 80.4 (76.6; 83.8)
  Yes258 18.5 (16.6; 20.7)92 19.6 (16.2; 23.4)
Smoking
  Not a smoker781 54.0 (51.4; 56.6)262 55.0 (50.5; 59.5)
  Smoker182 12.6 (11.0; 14.4)58 12.2 (9.5; 15.5)
  Former smoker483 33.4 (31.0; 35.9)156 32.8 (28.7; 37.1)
Alcohol consumption e
  No 1138 78.8 (76.6; 80.8)355 74.6 (70.5; 78.3)
  Yes307 21.2 (19.2; 23.4)121 25.4 (21.7; 29.5)
Multimorbidity
  Up to 4 diseases47335.3 (32.8; 37.9)17537.6 (33.3; 42.1)
  5 or more diseases86664.7 (62.1; 67.2) 29162.4 (57.9; 66.7)
Depression f
  No 1182 84.8 (82.8; 86.6)408 86.4 (83.0; 89.3)
  Yes212 15.2 (13.4; 17.2)64 13.6 (10.7; 17.0)
Polypharmacy g
  No 513 35.6 (33.1; 38.1)150 31.5 (27.5; 35.8)
  Yes929 64.4 (61.9; 66.9)326 68.5 (64.2; 72.5)
BMI h
  Low weight126 9.2 (7.8; 10.9)26 5.5 (3.8; 8.0)
  Normal471 34.5 (32.1; 37.1)152 32.1 (28.1; 36.4)
  Overweight767 56.3 (53.6; 58.8)295 62.4 (57.9; 66.6)
a Pearson’s chi-square test. b According to Associação Brasileira de Empresas de Pesquisa (ABEP) [21]: category A/B indicating higher socioeconomic status; c assessed using the Diet Quality Index for the Elderly (Índice de Qualidade da dieta do idoso—IDQ-I) [22]; d assessed by the International Physical Activity Questionnaire (IPAQ) [23]; e alcohol consumption in the last month; f according to the Geriatric Depressive Scale (GDS-10) [25,26]; g continuous use of five or more medications [27]; h cut-offs recommended by Lipschitz et al. [28].
Table 2. Gait Speed (GS) and Timed Up and Go (TUG) differences between the two assessments, according to sociodemographic, behavioral, and health-related variables. n = 476. Pelotas, Brazil.
Table 2. Gait Speed (GS) and Timed Up and Go (TUG) differences between the two assessments, according to sociodemographic, behavioral, and health-related variables. n = 476. Pelotas, Brazil.
VariablesGS
p-Value a
2019–2014 Difference (95% CI)
TUG
p-Value a
2019–2014 Difference (95% CI)
Sex
  Male
  Female
Age (completed years)
p = 0.023
−0.26 (−0.31; −0.22)
−0.20 (−0.23; −0.16)
p = 0.88
p = 0.32
2.62 (1.19; 4.05)
1.71 (0.66; 2.76)
p < 0.001
  60–69
  70–79
  80+
−0.22 (−0.25; −0.18)
−0.23 (−0.28; −0.18)
−0.24 (−0.34; −0.14)
0.98 (−0.09; 2.05)
2.63 (1.16; 4.10)
7.95 (4.91; 10.98)
Skin colorp = 0.70p = 0.20
  White−0.22 (−0.25; −0.19) 1.80 (0.85; 2.75)
  Other than white−0.23 (−0.30; −0.17)3.26 (1.25; 5.26)
Marital statusp = 0.035p = 0.35
  Married/with a partner−0.23 (−0.27; −0.20)2.30 (1.19; 3.41)
  Without a partner/separated −0.27 (−0.34; −0.20)2.86 (0.66; 5.06)
  Widow(er)−0.16 (−0.22; −0.11)1.02 (−0.69; 2.74)
Economic level bp = 0.06p = 0.004
  A/B−0.26 (−0.31; −0.22) 0.44 (−0.84; 1.72)
  C−0.21 (−0.24; −0.17)3.23 (2.18; 4.29)
  D/E−0.16 (−0.25; −0.08)2.68 (0.28; 5.08)
Education level (completed years)p = 0.019p = 0.14
  None
  1–7
  ≥8
−0.21 (−0.29; −0.13)
−0.19 (−0.23; −0.16)
−0.28 (−0.33; −0.23)
3.87 (1.38; 6.35)
2.22 (1.10; 3.35)
1.01 (−0.50; 2.51)
Current work situationp = 0.91p = 0.45
  No (unemployed)−0.22 (−0.28; −0.17)2.29 (1.36; 3.22)
  Yes (employed)−0.22 (−0.25; −0.19)1.55 (−0.14; 3.24)
Diet quality cp = 0.82p = 0.80
  Low−0.23 (−0.28; −0.19)2.21 (0.78; 3.63)
  Average−0.22 (−0.26; −0.18)2.44 (1.18; 3.71)
  High−0.21 (−0.26; −0.16)1.81 (0.44; 3.19)
Leisure-time physical activity (>150 min/week) dp = 0.72p = 0.017
  No −0.22 (−0.25; −0.19)2.67 (1.80; 3.54)
  Yes−0.23 (−0.30; −0.17)0.27 (−1.51; 2.04)
Smokingp = 0.72p = 0.93
  Not a smoker−0.21 (−0.25; −0.17)1.92 (0.77; 3.08)
  Smoker−0.24 (−0.32; −0.17)2.42 (−0.05; 4.88)
  Former smoker−0.23 (−0.28; −0.18)2.17 (0.66; 3.68)
Alcohol consumption ep = 0.045p = 0.11
  No −0.21 (−0.24; −0.17)2.48 (1.48; 3.47)
  Yes−0.27 (−0.32; −0.22)0.86 (−0.84; 2.56)
Multimorbidityp = 0.69p = 0.07
  Up to 4 diseases−0.22 (−0.26; −0.17)1.21 (−0.08; 2.50)
  5 or more diseases−0.23 (−0.26; −0.19)2.70 (1.71; 3.70)
Depression fp = 0.51p = 0.89
  No −0.23 (−0.26; −0.20)2.14 (1.30; 2.98)
  Yes−0.20 (−0.27; −0.13)2.31 (0.23; 4.38)
Polypharmacy gp = 0.22p = 0.34
  No −0.20 (−0.25; −0.15)1.44 (−0.11; 2.98)
  Yes−0.23 (−0.27; −0.20)2.34 (1.31; 3.38)
Body Mass Index hp = 0.33p = 0.007
  Low weight−0.18 (−0.29; −0.06)−3.14 (−6.71; 0.42)
  Normal−0.25 (−0.30; −0.20)1.65 (0.16; 3.15)
  Overweight−0.21 (−0.25; −0.18)2.71 (1.64; 3.78)
a p-value obtained through adjusted mixed linear models including variables according to hierarchical levels: 1st Level: sex, age, skin color, marital status, economic level, education, work status; 2nd Level: diet quality, physical activity, smoking, alcohol consumption; 3rd Level: multimorbidity, depression, polypharmacy, and nutritional status. b According to Associação Brasileira de Empresas de Pesquisa (ABEP) [21]: category A/B indicating higher socioeconomic status; c assessed using the Diet Quality Index for the Elderly (Índice de Qualidade da dieta do idoso—IDQ-I) [22]; d assessed by the International Physical Activity Questionnaire (IPAQ) [23]; e alcohol consumption in the last month; f according to the Geriatric Depressive Scale (GDS-10) [25,26]; g continuous use of five or more medications [27]; h cut-offs recommended by Lipschitz et al. [28].
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Gomes, D.R.d.P.; Santos, L.P.; Gonzalez, M.C.; Vieira, E.R.; Bielemann, R.M. Changes in Physical Performance among Community-Dwelling Older Adults in Six Years. Int. J. Environ. Res. Public Health 2023, 20, 5579. https://doi.org/10.3390/ijerph20085579

AMA Style

Gomes DRdP, Santos LP, Gonzalez MC, Vieira ER, Bielemann RM. Changes in Physical Performance among Community-Dwelling Older Adults in Six Years. International Journal of Environmental Research and Public Health. 2023; 20(8):5579. https://doi.org/10.3390/ijerph20085579

Chicago/Turabian Style

Gomes, Darlise Rodrigues dos Passos, Leonardo Pozza Santos, Maria Cristina Gonzalez, Edgar Ramos Vieira, and Renata Moraes Bielemann. 2023. "Changes in Physical Performance among Community-Dwelling Older Adults in Six Years" International Journal of Environmental Research and Public Health 20, no. 8: 5579. https://doi.org/10.3390/ijerph20085579

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